Final Flashcards
Complete dominance
The dominant allele has the same phenotypic effect whether present in one or two copies
Incomplete dominance
The appearance of the heterozygous hybrid falls between the phenotypes of the two homozygous parents
Codominance
Both alleles are expressed in heterozygous individuals and neither allele is masked by the other
(Different from incomplete dominance bc each trait in present separately)
(Ex. AB blood type)
Pleiotropy
One gene influences multiple characters
Ex. sickle cell anemia
Polygenic inheritance
Additive effects of two or more genes on a single phenotypic character
(Opposite of pleiotropy)
Law of independent assortment
Inheritance of one character has no effect on the inheritance of another
Each pair of alleles sorts independently of other pairs of alleles during gamete formation
Physical basis in the orientation of homologous chromosome pairs in metaphase I
Law of segregation
A sperm or egg cell carries only one allele for each inherited character bc alleles pairs separate during the production of gametes
Physical basis in the separation of homologues in anaphase I
Linked genes
Genes located on the same chromosome, close together tend to be inherited together
Do not follow law of independent assortment
wild type
The traits most common in nature
Recombinant
Coming from two or more sources
Testcross
a mating between an individual with an unknown genotype with an homozygous recessive individual
Dihybrid
Dihybrid cross
heterozygous for both characters (RrYy)
Crossing these individuals with one another
recombination frequency
Percentage of recombinant offspring in a generation
In linked genes, most offspring have parental phenotypes but some are recombinant (crossing over of heterozygous alleles)
alleles
alternative versions of genes
somatic cell
typical body cell containing 46 chromosomes
homologous chromosomes
a pair of matching chromosomes that are twins in length and centromere position, carry genes controlling the same inherited characteristics
two chromosomes of a homologous pair may have different versions of the same gene
locus
position on a chromosome where a particular gene is
autosomes
non sex chromosomes found in 22 pairs in all humans